CROSS-REFERENCE TO RELATED APPLICATION
[0001] This application claims priority to and the benefit of Korean Patent Application
No.
10-2017-0081451 filed in the Korean Intellectual Property Office on June 27, 2017, the entire contents
of which are incorporated herein by reference.
BACKGROUND OF THE INVENTION
(a) Field of the Invention
[0002] The present invention relates to an alloy-coated steel sheet and a manufacturing
method thereof.
[Background Art]
(b) Description of the Related Art
[0003] Iron is a metal which is the most widely used metal industrially due to rich resources,
excellent characteristics, and a low price. Despite these advantages of iron, there
is a disadvantage that corrosion occurs in the atmosphere. The corrosion of the iron
is a phenomenon in which iron ions are eluted when oxygen or water electrochemically
reacts with the iron, and when such a reaction proceeds, an oxide of iron (FeOOH)
is generated in an eluted portion, which is called rust. The rust of iron consists
of various stoichiometric oxides and hydroxides, and a feature in which oxidation
continuously occurs over time is one of the features of iron. The iron is processed
and used in various forms, and in the case of automobiles, construction materials
and household appliances, cold-rolled steel sheets, that is, cold rolled steel sheets
have been mainly used.
[0004] A representative method for preventing corrosion of the steel sheet is to plate other
metals on the surface of the steel sheet. Types of plated films may be divided into
a sacrificial corrosion prevention film and a blocking corrosion prevention film.
In the sacrificial corrosion prevention film, a metal such as zinc, magnesium, or
aluminum, in which oxidation is easier than iron and rust is easily generated, is
coated, and the coated metal is corroded preferentially to protect the steel sheet.
In the blocking corrosion prevention film, a metal such as lead or tin, which is more
difficult to be corroded than the steel sheet, is coated to block water and oxygen
from reaching iron.
[0005] In order to prevent the corrosion of the steel sheet, currently, zinc plating has
been most widely used. After a zinc-plated steel sheet is developed, various efforts
to improve corrosion resistance have been made and one of the efforts is to coat a
zinc alloy. A high corrosion resistant material system using an alloy includes Zn-AI,
Zn-Ni, Zn-Fe, Zn-Al-Mg, and the like. Such a zinc or zinc alloy-plated steel sheet
has been widely used for construction materials and household appliances including
automobiles.
[0006] Aluminum is also used for preventing corrosion of the steel sheet, and application
fields of aluminum are further various unlike zinc. An aluminum film has a beautiful
color and excellent corrosion resistance and heat resistance and thus has been used
for coating of conductive films of a semiconductor, protective films of magnetic materials
or steel sheets, and coating of hyperthermia system of appliances, mufflers for automobiles,
etc. in addition to decorative films such as cosmetic cases and accessories.
[0007] The aluminum film is manufactured by using a vacuum coating or electroplating or
hot dipping method. However, in the case of the electroplating, productivity is deteriorated
because the efficiency is low, and thus a hot-dip plating method and a vacuum coating
method have been mostly used.
[0008] The aluminum plated steel sheet has excellent corrosion resistance, while has a disadvantage
that when a defect occurs on the film, the corrosion intensively occurs at the defect
portion, and the reason is that aluminum has sacrificial corrosion prevention inferior
to zinc. Accordingly, in the case of the hot-dip aluminum plated steel sheet, the
thickness of the plated layer is increased to 15 microns (µm) or more to solve the
problems. In the hot-dip aluminum plated steel sheet, since the process is performed
at a high temperature, an Al-Fe-Si alloy is made at an interface, and thus there is
a disadvantage that workability is poor.
[0009] The aluminum film using vacuum coating has been applied in most applications by reducing
the thickness, and even in corrosion resistant coating, it is general to coat the
aluminum film with a thickness of about several microns. In the case of the aluminum
film, when the thickness is several microns or less, red rust is generated at about
72 hours in a salt spray test. Accordingly, improvement of characteristics is required
to apply aluminum to the steel sheet as corrosion resistant coating. Further, in the
case of the aluminum film, since a sacrificial corrosion prevention characteristic
is weak as compared to zinc, there is a disadvantage that once red rust is generated,
the red rust is entirely spread for a short time.
[0010] Therefore, researches for solving the problems as described above are urgent.
[0011] The above information disclosed in this Background section is only for enhancement
of understanding of the background of the invention and therefore it may contain information
that does not form the prior art that is already known in this country to a person
of ordinary skill in the art.
SUMMARY OF THE INVENTION
[Technical Problem]
[0012] An exemplary embodiment of the present invention is to provide an alloy-coated steel
sheet having a high corrosion resistant characteristic even in a small thickness by
forming a sacrificial corrosion prevention alloy-coated film on a steel sheet and
a manufacturing method thereof.
[0013] An alloy-coated steel sheet according to the present invention includes: a steel
sheet; and an Al-Mg-Si alloy layer disposed on the steel sheet, wherein the Al-Mg-Si
alloy layer has a form in which Mg-Si alloy grains are included in an alloy layer
consisting of an Al-Mg alloy phase.
[0014] The alloy-coated steel sheet may further include an Al-Si alloy layer disposed between
the steel sheet and the Al-Mg-Si alloy layer.
[0015] The Al-Mg-Si alloy layer may have a gradient of an Mg content in the alloy layer.
[0016] The Mg content in the Al-Mg-Si alloy layer may be 15 wt% or more and 90 wt% or less
with respect to total 100 wt% of the Al-Mg-Si alloy layer.
[0017] The Al-Mg alloy phase may include Al
3Mg
2 and Al
12Mg
17.
[0018] The Al-Mg alloy phase may include Al other than Al
3Mg
2 and Al
12Mg
17, and Mg applied to the Al.
[0019] The Mg-Si alloy grains may include Mg
2Si.
[0020] The Mg-Si alloy grains may be amorphous.
[0021] The content of Mg-Si alloy grains in the Al-Mg-Si alloy layer may be 1 wt% or more
and 70 wt% or less with respect to total 100 wt% of the Al-Mg-Si alloy layer.
[0022] The alloy-coated steel sheet may further include an Al-Fe-Si alloy layer disposed
between the steel sheet and the Al-Mg-Si alloy layer.
[0023] The alloy-coated steel sheet may further include an Mg layer; or an Al-Mg alloy layer
disposed on the Al-Mg-Si alloy layer.
[0024] A manufacturing method of an alloy-coated steel sheet according to the present invention
includes: preparing an aluminum plated steel sheet including a plated layer containing
Al and Si; forming an Mg coated layer by coating Mg on the aluminum plated steel sheet;
and diffusing Mg into the plated layer by heat-treating the aluminum plated steel
sheet coated with Mg to form an Al-Mg-Si alloy layer, wherein the Al-Mg-Si alloy layer
has a form in which Mg-Si alloy grains are included in an alloy layer consisting of
an Al-Mg alloy phase.
[0025] In the diffusing of Mg into the plated layer by heat-treating the aluminum plated
steel sheet coated with Mg, the aluminum plated steel sheet may be heat-treated at
a temperature of 300°C to 450°C.
[0026] In the diffusing of Mg into the plated layer by heat-treating the aluminum plated
steel sheet coated with Mg, the aluminum plated steel sheet may be heat-treated for
5 seconds to 600 seconds.
[0027] In the diffusing of Mg into the plated layer by heat-treating the aluminum plated
steel sheet coated with Mg, the Al-Mg alloy phase may be generated in the Al-Mg-Si
alloy layer, and the Al-Mg alloy phase may include Al
3Mg
2, and Al
12Mg
17.
[0028] In the diffusing of Mg into the plated layer by heat-treating the aluminum plated
steel sheet coated with Mg, the Mg-Si alloy grains may be generated in the Al-Mg-Si
alloy layer, and the Mg-Si alloy grains may include Mg
2Si.
[0029] The forming of the Mg coated layer by coating Mg on the aluminum plated steel sheet
may be performed by physical vapor deposition (PVD).
BRIEF DESCRIPTION OF THE DRAWINGS
[0030]
FIG. 1 is a schematic view of a continuous coating device which may be used for manufacturing
an alloy-coated steel sheet.
FIG. 2 is a schematic view of an alloy-coated steel sheet according to a first exemplary
embodiment of the present invention.
FIG. 3 is a schematic view of an alloy-coated steel sheet according to a second exemplary
embodiment of the present invention.
FIG. 4 is a scanning electron microscope (SEM) photograph before and after heat treatment
of a hot-dip aluminum plated steel sheet coated with Mg of Example 2.
FIG. 5 is an SEM photograph for an alloy-coated steel sheet of Example 4.
FIG. 6 is a glow discharge spectrometer analysis result for an alloy-coated steel
sheet of Example 5.
FIG. 7 is a glow discharge spectrometer analysis result for an alloy-coated steel
sheet of Example 6.
FIG. 8 is an SEM photograph for cross sections of a coated layer before heat treatment
and a coated layer heat-treated at 400°C for 120 seconds, 300 seconds, and 600 seconds.
FIG. 9 is an SEM photograph of observing diffusion of three elements of Al, Mg, and
Si according to a heat-treatment time on a coated layer surface.
FIG. 10 is a transmission electron microscope (TEM) photograph for an alloy-coated
steel sheet of Example 7.
FIG. 11 is a TEM photograph for an alloy-coated steel sheet of Example 8.
FIG. 12 is a TEM photograph for an alloy-coated steel sheet of Example 9.
FIG. 13 is a TEM photograph for an alloy-coated steel sheet of Comparative Example
4.
FIG. 14 is a result illustrating a volume fraction for each phase of an alloy-coated
steel sheet according to a heat-treatment time at a temperature of about 400°C.
FIG. 15 is X-Ray diffraction analysis results for alloy-coated steel sheets of Example
7, Example 8, Example 9, and Comparative Example 4.
FIG. 16 is a glow discharge spectrometer analysis result for an alloy-coated steel
sheet of Example 7.
FIG. 17 is a glow discharge spectrometer analysis result for an alloy-coated steel
sheet of Example 8.
FIG. 18 is a glow discharge spectrometer analysis result for an alloy-coated steel
sheet of Example 9.
FIG. 19 is a glow discharge spectrometer analysis result for an alloy-coated steel
sheet of Comparative Example 4.
FIG. 20 is a result of evaluating a surface corrosion resistance based on initial
red rust generation times of Example 7 (Type-1), Example 8 (Type-2), Example 9 (Type-3),
and Comparative Example 4 (NHT).
DETAILED DESCRIPTION OF THE EMBODIMENTS
[0031] Hereinafter, exemplary embodiments of the present invention will be described in
detail. However, the exemplary embodiments are proposed as an example, the present
invention is not limited thereto, and the present invention is just defined by a range
of claims to be described below.
[0032] Unless otherwise defined, all terms (including technical and scientific terms) used
in the present specification may be used as the meaning which may be commonly understood
by a person with ordinary skill in the art, to which the present invention belongs.
Throughout the specification, unless explicitly described to the contrary, the word
"comprise" and variations such as "comprises" or "comprising", will be understood
to imply the inclusion of stated elements but not the exclusion of any other elements.
Unless particularly stated otherwise in the present specification, a singular form
also includes a plural form.
[0033] In addition, since a size and a thickness of each configuration illustrated in the
drawings is arbitrarily shown for ease of description, the present invention is not
necessarily limited thereto.
[0034] Throughout the specification, it will be understood that when an element such as
a layer, a film, a region, or a substrate is referred to as being "on" the other element,
it can be directly on the other element or intervening elements may also be present.
[0035] Throughout the specification, it will be understood that when an element such as
a layer, a film, a region, or a substrate is referred to as being "above" or "on"
the other element, it is meant that the element is disposed on or below a target element
and it is not necessarily meant that the element is dispsoed on the upper side based
on a direction of gravity.
[0036] Throughout the specification, unless otherwise defined, an "A layer" includes a layer
including A as well as a layer consisting of only A.
[0037] Throughout the specification, unless otherwise defined, an "A-B alloy layer" includes
a layer including an A-B alloy as well as a layer consisting of only an A-B alloy.
[0038] Throughout this specification, unless otherwise defined, an "A-B-C alloy layer" includes
a layer including an A-B-C alloy as well as a layer consisting of only an A-B-C alloy.
[0039] Recently, in order to solve the problems of the hot-dip aluminum plated steel sheet
described in the background art, studies have been conducted to improve sacrificial
corrosion prevention together with corrosion resistance by adding magnesium to the
hot-dip aluminum plated steel sheet containing silicon.
[0040] For example, studies have been conducted to manufacture a coated steel sheet having
excellent corrosion resistance by manufacturing an Al-Mg-Si plated steel sheet by
hot-dip plating. However, in the case of manufacturing the steel sheet by hot-dip
plating, there is a problem in that there is a limit to a control of an Mg content
and in the case of a thin plating of 20 g/m
2 or less, there is a disadvantage in that the corrosion resistance is rapidly deteriorated.
Further, an Mg
2Si alloy phase is known to improve the corrosion resistance, but in this case, there
is a problem in that characteristics are improved only in a small range of abound
6% of Mg. The Al-Mg-Si plated steel sheet is known to have excellent corrosion resistance
because the Mg
2Si phase is formed on the plated layer. The Mg
2Si phase has been reported to improve the corrosion resistance of the Al-Mg-Si plated
steel sheet when an area ratio in the plated layer is 0.5 or more and 30% or less
and a long diameter of the Mg
2Si phase is 10 µm or less.
[0041] However, since the Al-Mg-Si plated steel sheet manufactured by the hot-dip plating
method has a limitation to the control of the Mg content due to the manufacturing
process, it is not easy to manufacture the Al-Mg-Si plated steel sheet having a predetermined
content or more of Mg content (about 15% or more). Due to the Mg content limitation
of the Al-Mg-Si plated steel sheet and a high processing temperature, it is difficult
to form an Al
3Mg
2 phase or an Al
12Mg
17 phase in the Al-Mg-Si alloy layer in addition to the Mg
2Si phase as an intermetallic compound.
[0042] As another example, there are studies on a method of forming an Al-Mg alloy layer
by depositing Mg while a substrate coated with aluminum is heated at 350°C or more
and 500°C or less in vacuum and a method of coating and then heat-treating Mg on the
hot-dip aluminum plated steel sheet by physical vapor deposition. However, in these
methods, since Mg is deposited on the substrate heated at a high temperature in vacuum,
the loss of steam may occur and characteristic change data in accordance with the
generation of an intermetallic compound or the intermetallic compound are not presented
with respect to an Al-Mg-Si layer.
[0043] The present invention is derived to solve the problems of the aforementioned hot-dip
aluminum plated steel sheet and the problems of the Al-Mg alloy steel sheet, and according
to the present invention, since Mg is coated on the hot-dip aluminum plated steel
sheet by a physical vapor deposition method, there is no limitation to the Mg content
control of the Al-Mg-Si coated layer and it is possible to manufacture a structure
of various coated layers.
[0044] Specifically, magnesium is deposited on the hot-dip aluminum plated steel sheet containing
silicon to form a multi-layered alloy-coated film through heat treatment, thereby
providing an alloy-coated steel sheet having a high corrosion resistance characteristic
even in a small thickness while providing sacrificial corrosion prevention.
[0045] Hereinafter, a manufacturing method of an alloy-coated steel sheet according to an
exemplary embodiment of the present invention and a manufactured alloy-coated steel
sheet will be described.
[0046] An exemplary embodiment of the present invention provides a manufacturing method
of an alloy-coated steel sheet including: preparing an aluminum plated steel sheet
including a plated layer containing Al and Si; coating Mg on the aluminum plated steel
sheet to form a Mg coated layer; and diffusing Mg to the plated layer by heat-treating
the aluminum plated steel sheet coated with Mg.
[0047] The steel sheet may be a cold rolled steel sheet. However, the steel sheet is not
limited thereto.
[0048] . The aluminum plated steel sheet may be a hot-dip aluminum plated steel sheet, and
specifically, may consist of Si: 8 wt% or more and 10 wt% or less; Al: 88 wt% or more
and 90 wt% or less; and a residual amount of Fe with respect to total 100 wt% of the
plated layer.
[0049] Further, the plated layer of the aluminum plated steel sheet may include an Al-Fe-Si
alloy layer and an Al-Si alloy layer formed when aluminum is plated, and the alloy
layers may be formed on the steel sheet in order of the Al-Fe-Si alloy layer and the
Al-Si alloy layer. The Al-Fe-Si alloy layer may be formed by diffusing Fe in the steel
sheet into the Al-Si plated layer when the Al plated steel sheet is manufactured.
[0050] The coating of the coating Mg on the aluminum plated steel sheet may be performed
by physical vapor deposition (PVD). More specifically, the coating may be performed
by electromagnetic levitation physical vapor deposition (EML-PVD). However, the coating
method is not limited thereto, and so long as Mg is able to be deposited by physical
methods such as an electron beam evaporator, a thermal evaporator, a sputtering source,
and a cathodic arc source, Mg may be coated by applying various methods.
[0051] The heat treatment method in the heat treating step may be performed by an inductive
heating apparatus, but is not limited thereto and other suitable heat-treatment means
may be applied. Further, when the heat treatment is performed by methods other than
the inductive heating method, a heat treatment temperature may vary according to a
heat treatment method. In the present invention, the heat treatment temperature may
be 300°C to 450°C and a heat treatment time may be in a range of 5 seconds to 600
seconds. Specifically, the heat treatment temperature may be 320°C to 430°C, 340°C
to 410°C, and 360°C to 390°C
[0052] Specifically, the heat treatment time may be 40 seconds to 550 seconds, 100 seconds
to 500 seconds, 150 seconds to 450 seconds, 200 seconds to 400 seconds, and 250 seconds
to 350 seconds.
[0053] In the diffusing of Mg into the plated layer by heat-treating the aluminum plated
steel sheet coated with Mg, the heat treatment may be performed at a temperature of
300°C to 450°C.
[0054] When the heat treatment temperature is less than 300°C, a lot of time is required
in the heat treatment process and thus the manufacturing efficiency is lowered and
Al-Mg and Mg-Si alloy phases are not sufficiently generated by the heat treatment
to lower a corrosion resistance improvement effect. When the heat treatment temperature
is more than 450°C, pores are generated on the plated layer and roughness of the surface
of the plated layer is increased to lower the corrosion resistance, and a color of
the plated layer becomes darker to deteriorate the productivity. Further, the amount
of the Mg-Si alloy phase is larger than that of the Al-Mg alloy phase to increase
the sacrificial corrosion prevention and thus there is a possibility of reducing the
overall corrosion resistance. Accordingly, it is reasonable that the heat treatment
temperature is controlled to 300°C to 450°C.
[0055] In the diffusing of Mg into the plated layer by heat-treating the aluminum plated
steel sheet coated with Mg, the heat treatment may be performed for 5 seconds to 600
seconds.
[0056] When the heat treatment time is less than 5 seconds, the Al-Mg and Mg-Si alloy phases
are not sufficiently generated to lower a corrosion resistance improvement effect.
When the heat treatment time is more than 600 seconds, the pores in the plated layer
and the surface roughness are increased and the sacrificial corrosion prevention becomes
too high due to an increase in Mg-Si alloy phase and thus the corrosion resistance
may be lowered. Accordingly, it is reasonable that the heat treatment time is controlled
to 5 seconds to 600 seconds.
[0057] In the diffusing of Mg into the plated layer by heat-treating the aluminum plated
steel sheet coated with Mg, while the heat treatment time passes 60 seconds or more,
the Al-Mg alloy phase is generated in the Al-Mg-Si alloy layer and the Al-Mg alloy
phase may include Al
3Mg
2 and Al
12Mg
17.
[0058] Meanwhile, when the heat treatment time passes 200 seconds or more, Mg-Si alloy grains
are generated in the Al-Mg-Si alloy layer and the Mg-Si alloy grains may contain Mg
2Si.
[0059] When the heat treatment time becomes 200 seconds or more, an Mg-Si alloy phase containing
Mg
2Si is generated and as a result, since both the Al-Mg alloy phase and the Mg-Si alloy
phase are formed, the corrosion resistance of the alloy-coated steel sheet may be
improved.
[0060] Effects on the corrosion resistance of the alloy-coated steel sheet according to
a heat treatment time will be confirmed through the following Examples and Comparative
Examples.
[0061] An apparatus of FIG. 1 is a schematic view of a continuous coating apparatus which
may be used for manufacturing an alloy-coated steel sheet. However, this is just an
example of the manufacturing method and is not limited thereto.
[0062] The apparatus is configured by a steel sheet supplying device 11 for supplying a
hot-dip aluminum plated steel sheet 17 in an atmosphere, an inverse magnetron sputtering
source 12 capable of pre-treating the steel sheet in vacuum, a physical vapor deposition
(PVD) device 13 for coating Mg after pre-treatment, an inductive heating device 14
capable of heat-treating the steel sheet discharged to the atmosphere, and a steel
sheet discharging device 15 for rewinding the heat-treated coated steel sheet again.
The PVD device 13 may be an electromagnetic levitation (EML) source. The inverse magnetron
sputtering source 12 and the PVD device 13 may be installed and operated in a vacuum
container 16.
[0063] An exemplary manufacturing method of the alloy-coated steel sheet using the apparatus
is as follows. First, the hot-dip aluminum plated steel sheet 17 is prepared and alkaline
degreasing may be performed to remove residual oils such as anti-rust oil smeared
on the surface of the steel sheet.
[0064] Thereafter, the steel sheet is supplied to the vacuum container 16 while being transferred
by the steel sheet supplying device 11. Next, the surface cleaning of the steel sheet
may be performed by applying power to the inverse magnetron sputtering source 12 installed
in the vacuum container 16.
[0065] After the cleaning is completed, while the steel sheet is continuously transferred,
Mg may be vacuum-coated on the Al plated layer by the EML source 13 installed in the
vacuum container 16.
[0066] After the coating is completed, the steel sheet is continuously transferred to be
discharged to the atmosphere, and then the steel sheet may be heat-treated at a predetermined
temperature for a predetermined time using the inductive heating device 14 in the
atmosphere.
[0067] After the heat treatment is completed, the steel sheet is continuously transferred
to obtain the manufactured alloy-coated steel sheet.
[0068] Hereinafter, the steel sheet manufactured by the aforementioned manufacturing method
will be described. Features of the coated steel sheet found by the present invention
are divided into four, and in this specification, the four features are referred to
as a first exemplary embodiment to a fourth exemplary embodiment. Hereinafter, the
first to fourth exemplary embodiments of the present invention will be described in
detail.
First Exemplary Embodiment
[0069] FIG. 2 is a schematic view of an alloy-coated steel sheet according to a first exemplary
embodiment of the present invention. When describing with reference to FIG. 2, an
alloy-coated steel sheet according to a first exemplary embodiment of the present
invention manufactured by the manufacturing method includes a steel sheet 21; and
an Al-Mg-Si alloy layer 23 disposed on the steel sheet 21, and the Al-Mg-Si alloy
layer 23 may have a form in which Mg-Si alloy grains 25 are included in an alloy layer
consisting of an Al-Mg alloy phase 24.
[0070] The Al-Mg-Si alloy layer 23 may have a form in which a mixed structure in which the
Mg-Si alloy grains 25 are surrounded by the Al-Mg alloy phase 24 is included.
[0071] Since the alloy-coated steel sheet is manufactured by coating magnesium on a hot-dip
aluminum plated steel sheet by a physical vapor deposition method, an Al-Mg-Si coated
layer having a higher magnesium content than an existing hot-dip plating method is
able to be manufactured. When the Al-Mg-Si plated steel sheet is manufactured by the
hot-dip plating method, there is a limit to a magnesium content control due to a process,
and thus it is difficult to manufacture the Al-Mg-Si plated steel sheet having a predetermined
content or more of magnesium (about 15% or more). Because of this, in the structure
of the plated layer, the Mg-Si alloy phase exists in a form of grains in the aluminum
plated layer. As a result, since the Mg-Si alloy phase in the form of grains is difficult
to be uniformly dispersed and distributed in the aluminum plated layer, there is a
limit in improving the corrosion resistance of the plated layer. Further, in the hot-dip
plating process, since the Mg content is limited, there is a problem in that the Al-Mg
alloy phase is not sufficiently generated and it is difficult to control a generation
location of the Mg-Si alloy phase.
[0072] Meanwhile, in the alloy-coated steel sheet according to the first exemplary embodiment
of the present invention, it is possible to manufacture the Al-Mg-Si coated layer
in which the Mg-Si alloy grains exist in the coated layer formed with the Al-Mg alloy
phase unlike the plated layer manufactured by the hot-dip plating method and it is
possible to implement sacrificial corrosion prevention and high corrosion resistance
characteristics as supported by the embodiments to be described below.
[0073] More specifically, the Al-Mg alloy phase may contain Al
3Mg
2, and the Mg-Si alloy grains may contain Mg
2Si. The Al-Mg alloy phase may further include an Al
12Mg
17 phase.
[0074] As such, the Al-Mg-Si alloy layer in which alloy grains of the Mg
2Si phase are included in the alloy layer including the Al
3Mg
2 phase is formed to improve the corrosion resistance of the plated steel sheet by
increasing the sacrificial corrosion prevention as supported by the embodiments to
be described below. As a result, even in a small thickness range, high corrosion resistance
may be exhibited.
[0075] The Al-Mg alloy phase may include Al other than Al
3Mg
2 and Al
12Mg
17 and Mg applied to the Al. Accordingly, pure metal contributes to improved corrosion
resistance in addition to the Al-Mg and Mg-Si alloy phases to expect an effect of
improving insufficient corrosion resistance and sacrificial corrosion prevention of
the hot-dip aluminum plated steel sheet.
[0076] The Mg-Si alloy grains may be amorphous. The amorphous Mg-Si alloy grains have a
large surface area to improve adhesion in the coated layer.
[0077] Further, the content of Mg-Si alloy grains in the Al-Mg-Si alloy layer may be 1 wt
% or more and 70 wt% or less with respect to total 100 wt% of the Al-Mg-Si alloy layer.
When an Al-Mg-Si single layer is formed, the content of Mg-Si alloy grains in the
alloy layer may be increased by the sufficient diffusion of Mg. When the content of
Mg-Si alloy grains is too small, the corrosion resistance may be slightly improved.
When the content of Mg-Si alloy grains is too large, the sacrificial corrosion prevention
is increased and thus the coated layer is consumed for a short time and as a result,
there is a problem in that the corrosion resistance is decreased.
[0078] The alloy-coated steel sheet may further include an Al-Fe-Si alloy layer 22 disposed
between the steel sheet 21 and the Al-Mg-Si alloy layer 23, which may be formed by
diffusing and introducing Fe in the steel sheet into the Al-Si plated layer when the
Al plated steel sheet is manufactured as described above. Alternatively, the Al-Fe-Si
alloy layer 22 may be formed by diffusing and introducing Fe in the steel sheet into
the Al-Si plated layer when Mg is coated and then heat-treated.
[0079] The Al-Fe-Si alloy layer and the Al-Mg-Si alloy layer may prevent corrosion in the
sequential manner. As a result, the Al-Fe-Si alloy layer and the Al-Mg-Si alloy layer
exhibit excellent corrosion resistance as compared to a general aluminum or zinc plated
layer which prevents corrosion by a physical prevention method or a single method
such as sacrificial corrosion prevention.
[0080] Further, the alloy-coated steel sheet may further include an Mg layer disposed on
the Al-Mg-Si alloy layer or an Al-Mg alloy layer formed according to Mg diffusion.
As a result, since the corrosion in the sequential manner is reinforced, it is possible
to exhibit excellent corrosion resistance.
Second Exemplary Embodiment
[0081] FIG. 3 is a schematic view of an alloy-coated steel sheet according to a second exemplary
embodiment of the present invention. When describing with reference to FIG. 3, an
alloy-coated steel sheet according to a second exemplary embodiment of the present
invention manufactured by the manufacturing method includes a steel sheet 21; an Al-Si
alloy layer 26 disposed on the steel sheet; and an Al-Mg-Si alloy layer 23 disposed
on the Al-Si alloy layer 26, and the Al-Mg-Si alloy layer 23 may have a form in which
Mg-Si alloy grains 25 are included in an alloy layer consisting of an Al-Mg alloy
phase 24.
[0082] The Al-Mg-Si alloy layer 23 may have a form in which a mixed structure in which the
Mg-Si alloy grains 25 are surrounded by the Al-Mg alloy phase 24 is included.
[0083] The description for the Al-Mg-Si alloy layer is the same as described in the first
exemplary embodiment and will be omitted.
[0084] The Al-Si alloy layer may be disposed between the steel sheet and the Al-Mg-Si alloy
layer. The Al-Si alloy layer may have existed in an Al hot-dip plated steel sheet,
and alternatively, may be newly formed by diffusing Al and Si toward the steel sheet
surface during the heat treatment in the manufacturing method.
[0085] As a result, the Al-Si alloy layer and the Al-Mg-Si alloy layer may prevent corrosion
in the sequential manner.
[0086] Furthermore, the alloy-coated steel sheet may further include an Al-Fe-Si alloy layer
22 disposed between the steel sheet 21 and the Al-Mg-Si alloy layer 23, which may
be formed by diffusing and introducing Fe in the steel sheet into the Al-Si plated
layer when the Al plated steel sheet is manufactured as described above. Alternatively,
the Al-Fe-Si alloy layer 22 may be formed by diffusing and introducing Fe in the steel
sheet into the Al-Si plated layer when Mg is coated and then heat-treated.
[0087] Accordingly, the Al-Fe-Si alloy layer, the Al-Si alloy layer, and the Al-Mg-Si alloy
layer may prevent corrosion in the sequential manner. As a result, the Al-Fe-Si alloy
layer, the Al-Si alloy layer, and the Al-Mg-Si alloy layer exhibit excellent corrosion
resistance as compared to a general aluminum or zinc plated layer which prevents corrosion
by a physical prevention method or a single method such as sacrificial corrosion prevention.
[0088] Further, the alloy-coated steel sheet may further include an Mg layer disposed on
the Al-Mg-Si alloy layer or an Al-Mg alloy layer formed according to Mg diffusion.
As a result, since the corrosion in the sequential manner is reinforced, it is possible
to exhibit excellent corrosion resistance.
[0089] Further, the content of Mg-Si alloy grains in the Al-Mg-Si alloy layer may be 1 wt
% or more and 50 wt% or less with respect to total 100 wt% of the Al-Mg-Si alloy layer.
When the content of Mg-Si alloy grains is too small, the corrosion resistance may
be slightly improved. When the content of Mg-Si alloy grains is too large, the sacrificial
corrosion prevention is increased and thus the coated layer is consumed for a short
time and as a result, there is a problem in that the corrosion resistance is decreased.
Third Exemplary Embodiment
[0090] When describing a third exemplary embodiment with reference to FIG. 2, an alloy-coated
steel sheet according to a third exemplary embodiment of the present invention manufactured
by the manufacturing method includes a steel sheet 21; and an Al-Mg-Si alloy layer
23 disposed on the steel sheet, and the Al-Mg-Si alloy layer 23 may have a gradient
of an Mg content in the alloy layer.
[0091] Since the alloy-coated steel sheet is manufactured by coating magnesium on a hot-dip
aluminum plated steel sheet by a physical vapor deposition method, there is no limit
to a magnesium content control of the Al-Mg-Si alloy layer unlike the related art
and the magnesium distribution may be controlled by diffusion heat-treatment and the
like, and thus it is possible to manufacture various structures of the Al-Mg-Si alloy
layer.
[0092] Since the content gradient of Mg in the Al-Mg-Si layer exists, various alloy phases
according to an Mg concentration exist to expect a corrosion resistance improvement
effect. Examples of various alloy phases may include Al
12Mg
17, Al
3Mg
2, Mg
2Si, and the like. When these alloy phases exist depending on the Mg concentration
gradient, each alloy phase forms a layered structure, and thus there may be an effect
of delaying the corrosion of the coated steel sheet.
[0093] Specifically, the gradient of the Mg content in the Al-Mg-Si alloy layer may have
a form in which the Mg content is decreased inward from the surface of the Al-Mg-Si
alloy layer.
[0094] Alternatively, the gradient of the Mg content in the Al-Mg-Si alloy layer may have
a form in which the Mg content is increased inward from the surface of the Al-Mg-Si
alloy layer.
[0095] Alternatively, a point in which the Mg content in the Al-Mg-Si alloy layer is maximum
is included, and the gradient of the Mg content in the Al-Mg-Si alloy layer may have
a form in which the Mg content is increased inward from the surface of the Al-Mg-Si
alloy layer and then decreased from the point in which the Mg content is maximum.
[0096] Alternatively, the Al-Mg-Si alloy layer includes a content constant portion where
the Mg content is constant inward from the surface of the alloy layer and the Mg content
may be increased from a point where the content constant portion ends.
[0097] Alternatively, the Al-Mg-Si alloy layer includes a content constant portion where
the Mg content is constant inward from the surface of the alloy layer and the Mg content
may be decreased from the point where the content constant portion ends.
[0098] As described above, according to the manufacturing method of the alloy-coated steel
sheet of the present invention, since there is no limit to a magnesium content control
of the Al-Mg-Si alloy layer and the magnesium distribution may be controlled by diffusion
heat-treatment and the like, it is possible to manufacture various structures of the
Al-Mg-Si alloy layer. Accordingly, unlike the hot-dip plated steel sheet in which
the Mg concentration is uniform, it is possible to manufacture an alloy layer having
a layered structure and to expect an effect of maximizing the corrosion resistance
by properly combining sacrificial corrosion prevention and blocking corrosion prevention.
[0099] Further, the present invention exhibits a high corrosion resistance characteristic
as supported by embodiments to be described below.
[0100] The alloy-coated steel sheet may further include an Al-Si alloy layer disposed between
the steel sheet and the Al-Mg-Si alloy layer.
[0101] The Al-Si alloy layer may have existed in an Al hot-dip plated steel sheet, and alternatively,
may be newly formed by diffusing Al and Si toward the steel sheet surface during the
heat treatment in the manufacturing method.
[0102] As a result, the Al-Si alloy layer and the Al-Mg-Si alloy layer may prevent corrosion
in the sequential manner.
[0103] Furthermore, the alloy-coated steel sheet may further include an Al-Fe-Si alloy layer
22 disposed between the steel sheet 21 and the Al-Mg-Si alloy layer 23, which may
be formed by diffusing and introducing Fe in the steel sheet into the Al-Si plated
layer when the Al plated steel sheet is manufactured as described above. Alternatively,
the Al-Fe-Si alloy layer 22 may be formed by diffusing and introducing Fe in the steel
sheet into the Al-Si plated layer when Mg is coated and then heat-treated.
[0104] Accordingly, the Al-Fe-Si alloy layer, the Al-Si alloy layer, and the Al-Mg-Si alloy
layer may prevent corrosion in the sequential manner. As a result, the Al-Fe-Si alloy
layer, the Al-Si alloy layer, and the Al-Mg-Si alloy layer exhibit excellent corrosion
resistance as compared to a general aluminum or zinc plated layer which prevents corrosion
by a physical prevention method or a single method such as sacrificial corrosion prevention.
[0105] Further, the alloy-coated steel sheet may further include an Mg layer disposed on
the Al-Mg-Si alloy layer or an Al-Mg alloy layer formed according to Mg diffusion.
As a result, since the corrosion in the sequential manner is reinforced, it is possible
to exhibit excellent corrosion resistance.
[0106] Further, the Al-Mg-Si alloy layer of the alloy-coated steel sheet may have a form
in which Mg-Si alloy grains are included in the alloy layer consisting of an Al-Mg
alloy phase.
[0107] Such a form also contributes to the improved corrosion resistance and the detailed
contents are as described above.
Fourth Exemplary Embodiment
[0108] When describing a fourth exemplary embodiment with reference to FIG. 2, an alloy-coated
steel sheet according to a fourth exemplary embodiment of the present invention manufactured
by the manufacturing method includes a steel sheet 21; and an Al-Mg-Si alloy layer
23 disposed on the steel sheet, and the Mg content in the Al-Mg-Si alloy layer 23
may be 15 wt% or more with respect to total 100 wt% of the Al-Mg-Si alloy layer. More
specifically, the Mg content may be 15 wt% or more and 90 wt% or less.
[0109] Since the alloy-coated steel sheet is manufactured by coating magnesium on a hot-dip
aluminum plated steel sheet by a physical vapor deposition method, an Al-Mg-Si coated
layer having a higher magnesium content than an existing hot-dip plating method is
able to be manufactured. When the Al-Mg-Si plated steel sheet is manufactured by the
hot-dip plating method, there is a limit to a magnesium content control due to a process,
and thus it is difficult to manufacture the Al-Mg-Si plated steel sheet having a predetermined
content or more of magnesium (about 15% or more).
[0110] On the contrary, in the alloy-coated steel sheet according to the fourth exemplary
embodiment of the present invention, unlike a plated layer manufactured by a hot-dip
plating method, there is no limit to the Mg content control and it is possible to
manufacture the Al-Mg-Si plated steel sheet having a high content of Mg. As a result,
it is possible to implement sacrificial corrosion prevention and high corrosion resistance
characteristics as supported by the embodiments to be described below.
[0111] The alloy-coated steel sheet may further include an Al-Si alloy layer disposed between
the steel sheet and the Al-Mg-Si alloy layer.
[0112] The Al-Si alloy layer may have existed in an Al hot-dip plated steel sheet, and alternatively,
may be newly formed by diffusing Al and Si toward the steel sheet surface during the
heat treatment in the manufacturing method.
[0113] As a result, the Al-Si alloy layer and the Al-Mg-Si alloy layer may prevent corrosion
in the sequential manner.
[0114] Furthermore, the alloy-coated steel sheet may further include an Al-Fe-Si alloy layer
22 disposed between the steel sheet 21 and the Al-Mg-Si alloy layer 23, which may
be formed by diffusing and introducing Fe in the steel sheet into the Al-Si plated
layer when the Al plated steel sheet is manufactured as described above. Alternatively,
the Al-Fe-Si alloy layer 22 may be formed by diffusing and introducing Fe in the steel
sheet into the Al-Si plated layer when Mg is coated and then heat-treated.
[0115] Accordingly, the Al-Fe-Si alloy layer, the Al-Si alloy layer, and the Al-Mg-Si alloy
layer may prevent corrosion in the sequential manner. As a result, the Al-Fe-Si alloy
layer, the Al-Si alloy layer, and the Al-Mg-Si alloy layer exhibit excellent corrosion
resistance as compared to a general aluminum or zinc plated layer which prevents corrosion
by a physical prevention method or a single method such as sacrificial corrosion prevention.
[0116] Further, the alloy-coated steel sheet may further include an Mg layer disposed on
the Al-Mg-Si alloy layer or an Al-Mg alloy layer formed according to Mg diffusion.
As a result, since the corrosion in the sequential manner is reinforced, it is possible
to exhibit excellent corrosion resistance.
[0117] Further, the Al-Mg-Si alloy layer of the alloy-coated steel sheet may have a form
in which Mg-Si alloy grains are included in the alloy layer consisting of an Al-Mg
alloy phase.
[0118] Such a form also contributes to the improved corrosion resistance and the detailed
contents are as described above.
[0119] Hereinafter, preferred Examples and Comparative Examples of the present invention
will be described. However, the following Examples are just preferred embodiments
of the present invention and the present invention is not limited to the following
Examples.
Examples: Manufacturing of alloy-coated steel sheet
Example 1
[0120] An Al plated layer containing 9 wt% of Si, 88 wt% of Al, and a residual amount of
Fe was formed on a cold rolled steel sheet with a single-sided plating amount of 15
g/m
2 to prepare a hot-dip aluminum plated steel sheet. A thickness of the Al plated layer
was about 5 µm.
[0121] Alkaline degreasing was performed to remove residual oils such as anti-rust oil smeared
on the surface of the steel sheet.
[0122] Thereafter, while the steel sheet was supplied to a vacuum container by a steel sheet
supplying device, the surface cleaning of the steel sheet was performed by an inverse
magnetron sputtering source installed in the vacuum container.
[0123] After the cleaning was completed, while the steel sheet was continuously transferred,
Mg was vacuum-coated on the Al plated layer with a thickness of 0.5 µm by an EML source
installed in the vacuum container.
[0124] After the coating was completed, the steel sheet was continuously transferred to
be discharged to the atmosphere, and then the steel sheet was heat-treated using an
inductive heating device in the atmosphere. The heat treatment temperature was 400°C
and the heat treatment time was 120 seconds, and after the heat treatment was completed,
the steel sheet was continuously transferred to obtain the manufactured alloy-coated
steel sheet.
Example 2
[0125] Example 2 was manufactured in the same manner as Example 1, but an alloy-coated steel
sheet heat-treated for 300 seconds was manufactured.
Example 3
[0126] Example 3 was manufactured in the same manner as Example 1, but an alloy-coated steel
sheet heat-treated for 600 seconds was manufactured.
Example 4
[0127] Example 4 was manufactured in the same manner as Example 1, but an Mg coated layer
was coated with a thickness of 1.5 µm and an alloy-coated steel sheet heat-treated
for 120 seconds was manufactured.
Example 5
[0128] Example 5 was manufactured in the same manner as Example 1, but an Mg coated layer
was coated with a thickness of 1.5 µm and an alloy-coated steel sheet heat-treated
for 300 seconds was manufactured.
Example 6
[0129] Example 6 was manufactured in the same manner as Example 1, but an Mg coated layer
was coated with a thickness of 1.5 µm and an alloy-coated steel sheet heat-treated
for 600 seconds was manufactured.
Comparative Example 1
[0130] An Al plated layer containing 9 wt% of Si, 88 wt% of Al, and a residual amount of
Fe was formed on a steel sheet with a single-sided plating amount of 15 g/m
2 to prepare a hot-dip aluminum plated steel sheet.
Comparative Example 2
[0131] An electric zinc-plated steel sheet of a single-sided plating amount of 40 g/m
2 was prepared.
Comparative Example 3
[0132] A hot-dip zinc-plated steel sheet of a single-sided plating amount of 137.5 g/m
2 was prepared.
Experimental Examples
Experimental Example 1: Observation of scanning electron microscope (SEM) photograph
[0133] FIG. 4 is a scanning electron microscope (SEM) photograph before and after heat treatment
of a hot-dip aluminum plated steel sheet coated with Mg of Example 2.
[0134] FIG. 4A is an SEM photograph of a steel sheet in which Mg is coated on a hot-dip
aluminum plated steel sheet and not heat-treated, in which a cold rolled steel sheet
51, an Al-Fe-Si alloy layer 52, an Al-Si alloy layer 53 and an Mg coated layer 54
may be divided.
[0135] FIG. 4B is an SEM photograph of Example 2 heat-treated, in which it may be confirmed
that Mg is diffused into the Al-Si alloy layer to form an Al-Mg-Si alloy layer 55.
[0136] FIG. 5 is a SEM photograph for an alloy-coated steel sheet manufactured in Example
4. A content of each component in the coated layer was indicated by a different line,
respectively. As can be seen in FIG. 5, it can be seen that the Mg content is highly
kept up to a predetermined depth from the surface of the Al-Mg-Si alloy layer and
then decreased toward an interface with the steel sheet. Further, it can be seen that
the Al-Si plated layer exists.
Experimental Example 2: Glow Discharge Spectrometer Analysis
[0137] With respect to the alloy-coated steel sheet manufactured in Example 5, components
of the coated layer formed on the steel sheet were analyzed using a glow discharge
spectrometer (Device Name: GDS 850A, Manufacturer: LECO).
[0138] The results thereof were illustrated in FIG. 6. As illustrated in FIG. 6, it can
be seen that Mg is diffused into the hot-dip aluminum plated layer through heat treatment.
Further, it can be seen that the Mg content is high on the surface of the Al-Mg-Si
alloy layer and then linearly decreased toward the interface with the steel sheet.
Further, it can be seen that the Mg content in the Al-Mg-Si alloy layer is 15 wt%
or more.
[0139] FIG. 7 is a glow discharge spectrometer analysis result for an alloy-coated steel
sheet manufactured in Example 6. As illustrated in FIG. 7, it can be seen that Mg
is diffused into the hot-dip aluminum plated layer through heat treatment. Further,
it can be seen that the Mg content is increased up to a predetermined depth from the
surface of the Al-Mg-Si alloy layer and then decreased toward the interface with the
steel sheet. Further, it can be seen that the Mg content in the Al-Mg-Si alloy layer
is 15 wt% or more.
Experimental Example 3: Evaluation of Corrosion Resistance
[0140] With respect to steel sheet specimens of Example 1 to 6 and Comparative Examples
1 to 3, surface corrosion resistance was evaluated based on initial red rust generation
times using a salt spray test (ASTM B-117) method. The results thereof were illustrated
in Table 1 below.
Table 1
Classific ation |
Plating material |
Plating amount (Single-side, g/m2) |
Coating material |
Coating thicknes s (µm) |
Heat treatment temperatur e (°C) |
Heat treatment time (second) |
Red rust generation time (hour) |
Exampl e 1 |
Al-Si |
15 |
Mg |
0.5 |
400 |
120 |
1008 |
Exampl e 2 |
Al-Si |
15 |
Mg |
0.5 |
400 |
300 |
1344 |
Exampl e 3 |
Al-Si |
15 |
Mg |
0.5 |
400 |
600 |
1176 |
Exampl e 4 |
Al-Si |
15 |
Mg |
1.5 |
400 |
120 |
1920 |
Exampl e 5 |
Al-Si |
15 |
Mg |
1.5 |
400 |
300 |
2448 |
Exampl e 6 |
Al-Si |
15 |
Mg |
1.5 |
400 |
600 |
2064 |
Exampl e 7 |
Al-Si |
15 |
Mg |
1.0 |
400 |
120 |
1440 |
Exampl e 8 |
Al-Si |
15 |
Mg |
1.0 |
400 |
300 |
2064 |
Exampl e 9 |
Al-Si |
15 |
Mg |
1.0 |
400 |
600 |
1920 |
Compar ative Exampl e 1 |
Al-Si |
15 |
- |
- |
- |
- |
192 |
Compar ative Exampl e 2 |
Zn |
40 |
- |
- |
- |
- |
48 |
Compar ative Exampl e 3 |
Zn |
137.5 |
- |
- |
- |
- |
288 |
Compar ative Exampl e 4 |
Al-Si |
15 |
Mg |
1.0 |
- |
- |
936 |
[0141] As can be seen in Table 1, in Comparative Examples 1 to 3, red rust was generated
even in less than 300 hours. On the contrary, it can be seen that Examples 1 to 6
have corrosion resistance at least three times to at most about 8 times larger than
Comparative Examples.
[0142] As a result, the alloy-coated steel sheet of the Al-Mg-Si alloy layer of the present
invention has very improved corrosion resistance as compared with an existing alloy-coated
steel sheet and is expected to be usefully applied to surface treatment of a product
requiring high corrosion resistance.
Examples: Comparison of changes depending on heat treatment condition
Example 7
[0143] Example 7 was manufactured in the same manner as Example 1, but an Mg coated layer
was coated with a thickness of 1.0 µm and an alloy-coated steel sheet heat-treated
for 120 seconds was manufactured.
Example 8
[0144] Example 8 was manufactured in the same manner as Example 1, but an Mg coated layer
was coated with a thickness of 1.0 µm and an alloy-coated steel sheet heat-treated
for 300 seconds was manufactured.
Example 9
[0145] Example 9 was manufactured in the same manner as Example 1, but an Mg coated layer
was coated with a thickness of 1.0 µm and an alloy-coated steel sheet heat-treated
for 600 seconds was manufactured.
Comparative Example 4
[0146] An alloy-coated steel sheet was manufactured in the same manner as Example 1, but
an Mg coated layer was coated with a thickness of 1.0 µm and heat treatment was not
separately performed.
Experimental Example
Experimental Example 4: Observation of Scanning Electron Microscope (SEM) photograph
[0147] FIG. 8 is an SEM photograph for cross sections of a coated layer before heat treatment
and a coated layer heat-treated at 400°C for 120 seconds, 300 seconds, and 600 seconds.
[0148] As illustrated in FIG. 8, before heat treatment, an Mg coated layer and a hot-dip
aluminum plated layer are clearly divided. It can be seen that Mg is diffused into
the hot-dip aluminum plated layer when the heat treatment starts, and it can be seen
that an Mg diffusion depth is also increased when the time is increased.
[0149] Until the heat treatment time is about 120 seconds, the diffusion depth of Mg is
lowered and thus only an Al-Mg alloy phase is formed and an Mg-Si alloy phase is not
formed. When the heat treatment is performed for about 300 seconds, it can be seen
that both the Al-Mg alloy phase and the Mg-Si alloy phase are formed and the diffusion
of Mg is not diffused to the entire hot-dip aluminum plated layer. When the heat treatment
is performed for about 600 seconds, it can be seen that Mg is diffused to the entire
plated layer to be alloyed.
[0150] The generation of the alloy phase depending on a change in heat treatment time described
above can be seen even on the coated layer, and FIG. 9 is a photograph of observing
diffusion of three elements of Al, Mg, and Si according to a heat-treatment time on
a coated layer surface by using a scanning electron microscope. As shown in FIG. 9,
it can be seen that on the coated layer surface without performing the heat treatment,
Al and Si are separated and Mg is coated to be evenly distributed on the surface.
[0151] When the heat treatment is performed for about 120 seconds, it may be observed that
Mg starts to be diffused to be similar to the distribution of Al, which is a phenomenon
occurring when an Al-Mg alloy phase is formed. When the heat treatment is performed
for about 300 seconds, it can be seen that Mg is coupled to Si and thus the distributions
of Mg and Si become similar to each other.
Experimental Example 5: Observation of Transmission Electron Microscope (TEM) Photograph
[0152] FIG. 10 is a TEM photograph for an alloy-coated steel sheet manufactured in Example
7. Mg was diffused by heat treatment for about 120 seconds. As a result, an Al-Mg
alloy layer was formed. An Mg-Si alloy phase was not formed.
[0153] FIG. 11 is a TEM photograph for an alloy-coated steel sheet manufactured in Example
8. Mg was diffused to the top of an Al-Si plated layer by heat treatment for about
300 seconds. An Al-Mg-Si alloy layer and an Al-Si plated layer are able to be divided.
In the Al-Mg-Si alloy layer, a mixed structure of an Al-Mg alloy phase and an Mg-Si
alloy phase may be observed.
[0154] Specifically, it can be seen that Mg-Si alloy grains containing Mg
2Si exist in a form to be surrounded by an Al-Mg alloy phase containing Al
3Mg
2 in the Al-Mg-Si alloy layer. Further, the Mg-Si alloy grains containing Mg
2Si may be observed in a form to be introduced to the Al-Si plated layer.
[0155] FIG. 12 is a TEM photograph for an alloy-coated steel sheet manufactured in Example
9. Mg was diffused to the bottom of an Al-Si plated layer by heat treatment for about
600 seconds. As a result, an Al-Mg-Si alloy layer and an Al-Si plated layer were not
divided. In an entire area of the Al-Mg-Si alloy layer, a mixed structure of an Al-Mg
alloy phase and an Mg-Si alloy phase is able to be observed.
[0156] FIG. 13 is a TEM photograph for an alloy-coated steel sheet manufactured in Comparative
Example 4. The diffusion of Mg without separate heat treatment did not occur. As a
result, an Al-Mg-Si alloy layer was not formed and a mixed structure of an Al-Mg alloy
phase and an Mg-Si alloy phase was not able to be observed.
Experimental Example 6: XRD analysis
[0157] With respect to alloy-coated steel sheets manufactured in Example 7, Example 8, Example
9 and Comparative Example 4, XRD analysis was performed by using an X-Ray diffraction
device (Device Name: D/MAX-2500V-PC, Manufacturer: Rigaku).
[0158] FIG. 14 is a graph showing contents of a metal and an alloy phase existing in a coated
layer as a percentage in an X-ray diffraction result of a specimen heat-treated for
600 seconds, 900 seconds, and 3600 seconds while changing a heat treatment time to
60 seconds to 480 seconds in units of 20 seconds.
[0159] As can be seen in FIG. 14, when the heat treatment is performed at a temperature
of about 400°C, until the heat treatment time is up to 180 seconds from 60 seconds,
an Al-Mg alloy phase is generated and as the heat treatment time is increased, a fraction
of the Al-Mg alloy phase is increased.
[0160] Until the heat treatment time is up to 540 seconds from 200 seconds, an Mg-Si alloy
phase is generated and as the heat treatment time is increased, a fraction of the
Mg-Si alloy phase is increased. When the heat treatment time is increased, it can
be seen that a fraction of pure metal is relatively decreased. It can be seen that
the coated layer heat-treated for 600 seconds or more reacts with pure metal to be
almost changed to the alloy phase, and it can be seen that a ratio change of the Al-Mg
alloy phase and the Mg-Si alloy phase does not occur.
[0161] FIG. 15 is X-Ray diffraction analysis results for Al-Mg-Si alloy layers of alloy-coated
steel sheets of Example 7, Example 8, Example 9, and Comparative Example 4.
[0162] In Example 7 in which the heat treatment for about 120 seconds is performed, an Al-Mg
alloy phase (Al
3Mg
2) is observed, but an Mg-Si alloy phase (Mg
2Si) is not observed. In Example 8 in which the heat treatment for about 300 seconds
is performed and Example 9 in which the heat treatment for about 600 seconds is performed,
the Al-Mg alloy phase (Al
3Mg
2) and the Mg-Si alloy phase (Mg
2Si) are shown.
[0163] In Comparative Example 4 in which the heat treatment is not performed, single phases
of Al, Mg, and Si exist, but the Al-Mg alloy phase and the Mg-Si alloy phase are not
shown.
Experimental Example 7: Glow Discharge Spectrometer Analysis
[0164] With respect to the alloy-coated steel sheets manufactured in Example 7, Example
8, Example 9, and Comparative Example 4, components of the coated layers formed on
the steel sheets were analyzed using a glow discharge spectrometer (Device Name: GDS
850A, Manufacturer: LECO).
[0165] FIG. 16 is a glow discharge spectrometer analysis result for an alloy-coated steel
sheet manufactured in Example 7. It can be seen that Mg is diffused to about 2.5 µm
from the surface of the alloy-coated steel sheet by heat treatment for about 120 seconds.
[0166] FIG. 17 is a glow discharge spectrometer analysis result for an alloy-coated steel
sheet manufactured in Example 8. It can be seen that Mg is diffused to about 6 µm
from the surface of the alloy-coated steel sheet by heat treatment for about 300 seconds.
[0167] FIG. 18 is a glow discharge spectrometer analysis result for an alloy-coated steel
sheet manufactured in Example 9. It can be seen that Mg is diffused to about 7 µm
from the surface of the alloy-coated steel sheet by heat treatment for about 600 seconds.
[0168] On the contrary, FIG. 19 is a glow discharge spectrometer analysis result for an
alloy-coated steel sheet manufactured in Comparative Example 4. Since the heat treatment
is not performed, Mg is not diffused, but just exists on the surface of the alloy-coated
steel sheet.
Experimental Example 8: Evaluation of Corrosion Resistance
[0169] With respect to alloy-coated steel sheet manufactured in Example 7, Example 8, Example
9 and Comparative Example 4, surface corrosion resistance was evaluated based on initial
red rust generation times using a salt spray test (ASTM B-117) method. The results
thereof were confirmed in FIG. 20. NHT corresponds to Comparative Example 4 as an
alloy-coated steel sheet in which a separate heat treatment is not performed and Type-1,
Type-2, and Type-3 correspond to Example 7, Example 8, and Example 9, respectively.
[0170] In Example 7, red rust was generated only after about 1440 hours elapsed. In Example
6, red rust was generated only after about 2064 hours elapsed. In Example 7, red rust
was generated only after about 1920 hours elapsed.
[0171] On the contrary, in Comparative Example 4, red rust was generated after about 936
hours elapsed.
[0172] The present invention is not limited to the exemplary embodiments and may be prepared
in various different forms, and it will be understood by a person with ordinary skill
in the art, to which the present invention pertains, that the exemplary embodiments
of the present invention may be implemented in other specific forms without modifying
the technical spirit or essential feature of the present invention. Therefore, it
will be understood that the aforementioned exempalry embodiments are all illustrative
and are not restricted to a limited form.
<Descrition of symbols>
11: |
Steel sheet supply device |
12: |
Inverse magnetron sputtering source |
13: |
Physical vapor deposition device |
14: |
Inductive heating device |
15: |
Steel sheet discharging device |
16: |
Vacuum container |
17: |
Hot-dip aluminum plated steel sheet |
21: |
Steel sheet |
22: |
Al-Si-Fe alloy layer |
23: |
Al-Mg-Si alloy layer |
24: |
Al-Mg alloy phase |
25: |
Mg-Si alloy phase |
26: |
Al-Si alloy layer |
41: |
Aluminum (Al) |
42: |
Magnesium (Mg) |
43: |
Silicon (Si) |
44: |
Iron (Fe) |
51: |
Cold rolled steel sheet |
52: |
Al-Fe-Si alloy layer |
53: |
Al-Si alloy layer |
54: |
Mg layer |
55: |
Al-Mg-Si alloy layer |
[0173] While this invention has been described in connection with what is presently considered
to be practical exemplary embodiments, it is to be understood that the invention is
not limited to the disclosed embodiments. On the contrary, it is intended to cover
various modifications and equivalent arrangements included within the spirit and scope
of the appended claims.